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Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Stuart BD, Choi J, Zaidi S, Xing C, Holohan B, Chen R, Choi M, Dharwadkar P, Torres F, Girod CE, Weissler J, Fitzgerald J, Kershaw C, Klesney-Tait J, Mageto Y, Shay JW, Ji W, Bilguvar K, Mane S, Lifton RP, Garcia CK. Stuart BD, et al. Among authors: shay jw. Nat Genet. 2015 May;47(5):512-7. doi: 10.1038/ng.3278. Epub 2015 Apr 13. Nat Genet. 2015. PMID: 25848748 Free PMC article.
Adult-onset pulmonary fibrosis caused by mutations in telomerase.
Tsakiri KD, Cronkhite JT, Kuan PJ, Xing C, Raghu G, Weissler JC, Rosenblatt RL, Shay JW, Garcia CK. Tsakiri KD, et al. Among authors: shay jw. Proc Natl Acad Sci U S A. 2007 May 1;104(18):7552-7. doi: 10.1073/pnas.0701009104. Epub 2007 Apr 25. Proc Natl Acad Sci U S A. 2007. PMID: 17460043 Free PMC article.
Perifosine as a potential novel anti-telomerase therapy.
Holohan B, Hagiopian MM, Lai TP, Huang E, Friedman DR, Wright WE, Shay JW. Holohan B, et al. Among authors: shay jw. Oncotarget. 2015 Sep 8;6(26):21816-26. doi: 10.18632/oncotarget.5200. Oncotarget. 2015. PMID: 26307677 Free PMC article.
544 results